Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273505Generated: October 25, 2026

Dichloromethane → 7-(2-Chloro-5-methoxyphenyl)-5-methylbenzo[e][1,2,4]triazin-3-amine

https://huagongshe.com/reaction/273505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant7-Bromo-5-methylbenzo[e][1,2,4]triazin-3-amineHCID 24822752—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDimethoxyethane ethanol waterHCID 86587095—
Product7-(2-Chloro-5-methoxyphenyl)-5-methylbenzo[e][1,2,4]triazin-3-amineHCID 24822753—

Reaction Conditions

Temperature100 °C

Reaction Steps

7-bromo-5-methyl-benzo[1,2,4]triazin-3-ylamine (33.47 mmol, 1.0 equiv), 1-chloro-4-methoxy-2-boronic acid (50.21 mmol, 1.5 equiv), Pd(PPH3)4 (3.347 mmol, 0.1 equiv), and Na2CO3 (133.9 mmol, 4.0 equiv) were dissolved in DME/EtOH/water 6:1:1 and refluxed at 100° C. under an argon blanket for 4 h. The reaction was cooled to room temperature, diluted with 100 mL DCM and filtered. The precipitate that was recovered was suspended in water, filtered and rinsed with ether. The precipitate afforded 7-(2-chloro-5-methoxy-phenyl)-5-methyl-benzo[1,2,4]triazin-3-ylamine, as a green solid (8.37 g, 84% yield). Rf=0.85 (9:1 DCM/MeOH). 1H NMR (DMSO-d6): δ 3.35 (s, 6H), 7.01 (dd, J=8.8 Hz, J=3.0, 1H), 7.09 (d, J=3.0 Hz, 1H), 7.48 (d, J=8.8 Hz, 1H), 7.75 (bm, 2H). MS (ES+) m/z=303. LC retention time 3.03 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456176B2
Source datasetuspto-grants-2008_11
ORD IDord-2554428ba5d54cd4a7d3ae2361dc0a0c
Source noteuspto-grants-2008_11